Gustave Roussy, Université Paris-Saclay, Drug Development Department (DITEP), Villejuif; Laboratory for Immunomonitoring in Oncology (LIO), University Paris-Saclay, Gustave Roussy Cancer Campus, Villejuif.
Human and Social Sciences Department, Centre Léon Bérard, Lyon.
ESMO Open. 2022 Jun;7(3):100468. doi: 10.1016/j.esmoop.2022.100468. Epub 2022 May 6.
Access to clinical trials and especially early-phase trials (ECT) is an important issue in geriatric oncology. As cancer can be considered an age-related disease because the incidence of most cancers increases with age, new drugs should also be evaluated in older patients to assess their safety and efficacy. The EGALICAN-2 study was primarily designed to identify social and/or regional inequalities regarding access to ECT. We focused on the factors of inequalities in access to ECT in older patients.
During a 1-year period (2015-2016), a survey was conducted in 11 early-phase units certified by the French National Cancer Institute.
A total of 1319 patients were included in the analyses: 1086 patients (82.3%) were <70 years and 233 patients (17.7%) were >70 years. The most common tumor types at referral in older patients were gastrointestinal (19.3%), hematological (19.3%), and thoracic tumors (18.0%). Most patients referred to the phase I unit had signed informed consent and the rate was similar across age (92.7% in younger patients versus 90.6% in older patients; P = 0.266). The rate of screening failure was also similar across age (28.5% in younger patients versus 24.3% in older patients; P = 0.219). Finally, in older patients, univariate analyses showed that initial care received in the hospital having a phase I unit was statistically associated with first study drug administration (odds ratio 0.49, 90% confidence interval 0.27-0.88; P = 0.045).
Older patients are underrepresented in early clinical trials with 17.7% of patients aged ≥70 years compared with the number of new cases of cancer in France (50%). However, when invited to participate, older patients were prone to sign informed consent.
临床试验,尤其是早期临床试验(ECT)的可及性是老年肿瘤学中的一个重要问题。由于癌症可以被视为一种与年龄相关的疾病,因为大多数癌症的发病率随着年龄的增长而增加,因此也应该在老年患者中评估新药物,以评估其安全性和疗效。EGALICAN-2 研究主要旨在确定ECT 可及性方面的社会和/或区域不平等问题。我们专注于老年患者ECT 可及性不平等的因素。
在为期 1 年的时间内(2015-2016 年),在 11 个由法国国家癌症研究所认证的早期阶段单位进行了一项调查。
共有 1319 名患者纳入分析:1086 名患者(82.3%)<70 岁,233 名患者(17.7%)>70 岁。在老年患者中,最常见的转诊肿瘤类型是胃肠道(19.3%)、血液学(19.3%)和胸部肿瘤(18.0%)。大多数转诊至 I 期病房的患者已签署知情同意书,且年龄之间的同意率相似(年轻患者为 92.7%,老年患者为 90.6%;P=0.266)。筛选失败率在年龄之间也相似(年轻患者为 28.5%,老年患者为 24.3%;P=0.219)。最后,在老年患者中,单因素分析显示,在有 I 期病房的医院接受初始治疗与首次研究药物给药呈统计学相关(优势比 0.49,90%置信区间 0.27-0.88;P=0.045)。
与法国新癌症病例数(50%)相比,70 岁及以上的患者仅占早期临床试验的 17.7%,老年患者在早期临床试验中的代表性不足。然而,当被邀请参与时,老年患者更倾向于签署知情同意书。